Chenodal

Product NDC: 45043-876
11-digit product format: 450430876
Labeler code: 45043
Product ID: 45043-876_d6369783-3cd7-4d99-8ddd-07102a5512f9
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Chenodiol
Dosage form: TABLET, FILM COATED
Route: ORAL
Labeler: Manchester Pharmaceuticals Inc.
Application: ANDA091019
Marketing category: ANDA
Marketing start: 2009-10-01
Marketing end: 0000-00-00
Substance: CHENODIOL
Active strength: 250 mg/1
NDC exclude flag: E
Listing certified through: 2017-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
45043-876-40	2026-01-06	C162847	48780-1	956f9ecf-de24-621f-e053-dbdaa90a74ad	b8b4539b-31d1-40cb-b284-86cf8b16522a
45043-876-40	2019-10-21	C162847	48780-1	956f9ecf-de24-621f-e053-dbdaa90a74ad	b8b4539b-31d1-40cb-b284-86cf8b16522a

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
45043-876-40	EA - Each	45043-876	12606ba9-8fce-4689-9473-baabb4d09588	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version	Uploaded
Chenodiol	ACTIVE INGREDIENT	0GEI24LG0J	CHENODAL (CHENODIOL) TABLET, FILM COATED [MANCHESTER PHARMACEUTICALS INC.]	2
Chenodiol	ACTIVE MOIETY	0GEI24LG0J	CHENODAL (CHENODIOL) TABLET, FILM COATED [MANCHESTER PHARMACEUTICALS INC.]	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
45043-876	CHENODAL (CHENODIOL) TABLET, FILM COATED [MANCHESTER PHARMACEUTICALS INC.]	2	Legacy NDC	20100108_b8b4539b-31d1-40cb-b284-86cf8b16522a.zip